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Biochimica Et Biophysica Acta|December 13, 1983
Decreased ganglioside neuraminidase activity in fibroblasts from mucopolysaccharidosis patients. Inhibition of the activity in vitro by sulfated glycosaminoglycans and other compoundsJ Baumkötter, M CantzThe Biochemical Journal|February 15, 1988
Defective lysosomal release of glycoprotein-derived sialic acid in fibroblasts from patients with sialic acid storage diseaseK Mendla, J Baumkötter, C Rosenau, et al.Neuropediatrics|May 1, 1985
Familial lysosomal storage disease with generalized vacuolization and sialic aciduria. Sporadic Salla diseaseK Wolburg-Buchholz, W Schlote, J Baumkötter, et al.Journal of Inherited Metabolic Disease|July 4, 2006
Maple syrup urine disease: favourable effect of early diagnosis by newborn screening on the neonatal course of the diseaseE Simon, R Fingerhut, J Baumkötter, et al.Human Genetics|January 1, 1985
N-Acetylneuraminic acid storage diseaseJ Baumkötter, M Cantz, K Mendla, et al.European Journal of Pediatrics|October 5, 2001
"Adult" form of muscular carnitine palmitoyltransferase II deficiency: manifestation in a 2-year-old childK Gempel, C von Praun, J Baumkötter, et al.Prenatal Diagnosis|November 1, 1986
Prenatal diagnosis and confirmation of infantile sialic acid storage diseaseE Vamos, J Libert, N Elkhazen, et al.Pageof 1